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- 详细信息
- 文献和实验
- 技术资料
- 保存条件:
常温
- 保质期:
三年
- 英文名:
pTet-Off-Advanced
- 库存:
60
- 供应商:
信裕生物
- 规格:
5ug质粒
基本信息
| 质粒类型: | 四环素调控系统 |
|---|---|
| 启动子: | CMV |
| 克隆方法: | 多克隆位点,限制性内切酶 |
| 载体大小: | 7140 bp (查看载体序列) |
| 载体抗性: | Ampicillin (氨苄青霉素) |
| 筛选标记: | Neomycin (新霉素) |
订购信息
| 产品编号 | 产品名称 | 规格 | 价格 |
|---|---|---|---|
| XY1722 | pTet-Off-Advanced | 5ug质粒 |
¥1500.00 |
质粒图谱
载体描述
pTet-Off-Advanced expresses an improved version of the Tet (tetracycline)-controlled transactivator protein called tTA-Advanced (1–4). It is expressed to higher levels than the original tTA used in the Tet-Off® System (2). The tTA-Advanced protein is a fusion of amino acids 1–207 of the Tet repressor (TetR) and 39 amino acids containing three minimal "F"-type transcriptional activation domains (ADs) from the VP16 protein of herpes simplex virus. The gene is fully synthetic, lacks cryptic splice sites in the mRNA, and utilizes human codon preferences for stable expression in mammalian cells.
载体应用
The pTet-Off-Advanced Vector is used to develop stable Tet-Off Advanced cell lines, which are hosts for a tetracycline-controlled gene expression system. Once a vector containing a gene of interest under the control of a Tet-responsive element (e.g., TRE-Tight or TRE2) is transfected into a Tet-Off Advanced stable cell line, tTA-Advanced binds to the TRE in the absence of doxycycline (Dox, a tetracycline derivative), and activates transcription of the gene of interest to a very high level. In the presence of Dox, tTA-Advanced is unable to bind the TRE in a Tet-responsive promoter and the system is inactive. Additional information on TRE-containing vectors and protocols describing how to construct a Tet-Off Advanced cell line can be found in the Tet-Off Advanced Inducible Gene Expression System User Manual (PT3945-1).
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文献和实验。该系统发挥作用的机制如图所示。 Tet―on和Tet―off系统的作用机制采用该系统进行条件性基因敲除时,要将受特异性启动子调控的tTA的表达载体转入小鼠体内,同时还要将受Ptet 启动子调控的Cre重组酶的表达载体也转入小鼠体内。这样一个转基因小鼠与loxP的转基因小鼠进行交配,产生的子代小鼠中会在特定组织和器官中表达tTA,tTA再与Ptet 结合后激活下游的Cre重组酶的表达,实现特定基因在特定组织器官中的敲除。如果在子代小鼠出生时就给予四环素,并且一直维持下去,特定基因的敲除
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